All individuals with variants in gene OPTN

12 entries on 1 page. Showing entries 1 - 12.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

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Owner     
00078536 26740678-FamPatII1 PubMed: Goldstein 2016, Journal: Goldstein 2016 2-generation family, affected father, 4 sisters F - Morocco Jewish 46y - - - ALS upper motor neuron involvement (HP:0002493), no cognitive involvement (-HP:0100543) 1 5 Jamie Zeegers
00078537 26740678-FamPatII2 PubMed: Goldstein 2016, Journal: Goldstein 2016 - F - Morocco Jewish 43y - - - ALS upper motor neuron involvement (HP:0002493), no cognitive involvement (-HP:0100543) 1 1 Jamie Zeegers
00078538 26740678-FamPatII4 PubMed: Goldstein 2016, Journal: Goldstein 2016 PatII4 F - Morocco Jewish 52y - - - ALS rapidly progressive presenile dementia (HP:0000726), motor neuron damage (HP:0002493) 1 1 Jamie Zeegers
00078539 26740678-FamPatII5 PubMed: Goldstein 2016, Journal: Goldstein 2016 PatII5 F - Morocco Jewish >70y - - - Healthy/Control - 1 1 Jamie Zeegers
00226588 - - - - - - - - - - - ALS - 1 1 Aritoshi Iida
00363793 G542 PubMed: Huang 2014 - M - China - - - - - glaucoma see paper; ... 1 1 LOVD
00390785 - PubMed: Booij-2011 - - - - - - - - - retinal disease - 2 1 LOVD
00397528 190239 - - M no Germany - - - - - ALS12 Skeletal muscle atrophy, Muscle weakness, Proximal muscle weakness, Elevated circulating creatine kinase concentration, Polyneuropathy, Sensory axonal neuropathy, Peripheral axonal neuropathy, Peripheral neuropathy, Calcium channel antibody positivity, Autoimmunity ; father with ALS 1 1 Andreas Laner
00407038 OPTN#1 PubMed: Jiang 2022 family, 4 affected M yes China - - - - - ALS site onset limb 1 4 Johan den Dunnen
00407039 OPTN#2 PubMed: Jiang 2022 - F yes China - - - - - ALS - 1 1 Johan den Dunnen
00407040 OPTN#3 PubMed: Jiang 2022 - M - China - - - - - ALS site onset bulbar 2 2 Johan den Dunnen
00415652 I:1, I:4, II:5, II:7, II:10 PubMed: Mackay 2015 - - - - African-American - - - - retinal disease significantly elevated intra ocular pressure (IOP) >30 mm Hg with consistent visual field and/or optic nerve abnormalities. 1 5 LOVD
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